result 18181 件
JaLCDOI | 10.18926/AMO/32011 |
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FullText URL | fulltext.pdf |
Author | Futagami, Koujiro| Hirano, Naofumi| Iimori, Emiko| Motomura, Kenichi| Ide, Michiko| Kataoka, Yasuhumi| Araki, Hiroaki| Gomita, Yutaka| Oishi, Ryozo| |
Abstract | Non-traumatic rhabdomyolysis associated with organophosphate intoxication has not been generally reported. We report here in a severe case of fenitrothion poisoning complicated by rhabdomyolysis. A 43-year-old woman ingested approximately 100 ml of fenitrothion emulsion (50%) in an attempt to commit suicide. On day 3 after admission, her creatine phosphokinase (CPK) peaked at 47,762 IU/L. She received supportive treatment included sodium bicarbonate and fluid resuscitation. However, muscarinic symptoms including excessive miosis and salivation developed on day 5 when her CPK levels decreased. The delay in cholinergic symptoms might have been due to the trihexyphenidyl she took with the antipsychotic drugs. Fortunately, the present patient recovered from the acute cholinergic crisis, and acute renal failure was prevented by early diagnosis. This is a case of organophosphate poisoning complicated by rhabdomyolysis in a psychiatric patient. The masking of acute cholinergic symptoms should be taken into consideration in such patients. |
Keywords | fenitrothion organophosphate poisoning rhabdomyolysis psychiatric patient |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 129 |
End Page | 132 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332199 |
Web of Science KeyUT | 000168195700009 |
JaLCDOI | 10.18926/AMO/32010 |
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FullText URL | fulltext.pdf |
Author | Engelborghs, Sebastiaan| |
Abstract | With the development of new treatments, there is an increasing need for early diagnosis of sporadic Alzheimer's disease. Therefore, biological markers allowing positive diagnosis early in the course of the disease are highly desirable. Cerebrospinal fluid levels of protein tau were shown to be significantly increased in patients with Alzheimer's disease. Although sensitivity is high, poor specificity limits the diagnostic value of this marker. The same is true for the 42 amino acid isoform of beta-amyloid protein that is significantly decreased in cerebrospinal fluid of Alzheimer's disease patients. However, combining both markers could improve specificity at least allowing differentiation between Alzheimer's disease, normal ageing and depressive pseudodementia. Other biological markers such as cerebrospinal fluid levels of neurotransmitters, cytokines or superoxide dismutase were shown to have even less diagnostic value. The apolipoprotein epsilon 4 allele is a risk factor for Alzheimer's disease but not a diagnostic marker as many individuals who inherit epsilon 4 do not develop the disease. Till now, a single diagnostic marker allowing discrimination between Alzheimer's disease and other dementias does not exist. Combined cerebrospinal fluid levels of beta-amyloid protein and tau protein might be used as a marker that helps discriminating Alzheimer's disease from normal ageing and depression. |
Keywords | alzheimer's disease dementia marker neurochemistry cerebrospinal fluid |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 55 |
End Page | 63 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332200 |
Web of Science KeyUT | 000168195700001 |
JaLCDOI | 10.18926/AMO/32009 |
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FullText URL | fulltext.pdf |
Author | Ohke, Masashi| Tada, Shinya| Nabe, Makoto| Matsuo, Kiyoshi| Kataoka, Mikio| Harada, Mine| |
Abstract | Allergic and chronic inflammation of the airway is regarded as the main pathogenesis of bronchial asthma, in which adhesion of inflammatory cells requires the expression of adhesion molecules. Thus, to clarify the role of fibronectin (FN) in the airway inflammation of bronchial asthma, FN levels in plasma and bronchoalveolar lavage fluid (BALF) from bronchial asthmatics were determined. FN concentrations in plasma and BALF were measured by enzyme-linked immunosorvent assay (ELISA) in 17 asthmatic patients and 10 healthy controls to elucidate the role of FN in allergic inflammation. The mean FN/albumin (Alb) level in the BALF of asthmatic patients was 2.973 micrograms/mg, which was significantly higher than that of healthy controls (0.727 microgram/mg). Non-atopic asthmatics showed a significantly higher level of FN in their BALF in comparison with atopic asthmatics, although the ratio of FN to albumin showed no significant difference. FN levels in BALF correlated significantly with total cell density (r = 0.71, P < 0.05) and alveolar macrophage density (r = 0.64, P < 0.05). FN levels in plasma did not correlate with those in BALF. In conclusion, increased FN in BALF, which was produced locally in the airways of asthmatic patients, is actively involved in the regulation of allergic inflammation. |
Keywords | airway inflammation adhesion molecule bronchoalveolar lavage fluid bronchial asthma fibronectin |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 83 |
End Page | 89 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332203 |
Web of Science KeyUT | 000168195700004 |
JaLCDOI | 10.18926/AMO/32008 |
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FullText URL | fulltext.pdf |
Author | Ishikura, Takashi| |
Abstract | The biomechanics of using a walker for the partial weight bearing gait and as a method for gradually increasing the muscle activation level were examined with a force plate and surface electromyography. The results showed that the weight bearing force during gait with a walker is determined by the flexion angle of the hip joint. The value remains constant for each stride, indicating that a walker can be used for the partial weight bearing gait. Moreover, the muscle activation levels in the rectus femoris muscle and biceps femoris muscle per unit time during normal gait and gait with a walker with varying hip joint flexion angles were found to be correlated with the weight bearing force and to be constant for each stride. In addition, the muscle activation level was consistent with the level observed during the open kinetic chain resistance exercise with a specific loading level. These findings suggest that normal gait and gait with a walker may be applicable as a method for gradually increasing the muscle activation level. |
Keywords | gait with a walker ground reaction force integrated electromyogram partial weight bearing gait muscle activation level |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 73 |
End Page | 82 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332202 |
Web of Science KeyUT | 000168195700003 |
JaLCDOI | 10.18926/AMO/32007 |
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FullText URL | fulltext.pdf |
Author | Furusato, Shoji| Takahashi, Tomohiro| Mori, Sadao| Takahashi, Yasuo| Tsuda, Toshihiko| Namba, Masayoshi| Mochizuki, Hidenori| |
Abstract | CD14 is a pattern recognition receptor on myeloid cells and plays a pivotal role in an innate immune system that is responsible for Gram-negative and Gram-positive bacteria infection. Lipopolysaccharide (LPS), a cell wall component of Gram-negative bacteria, can induce production of a large quantity of proinflammatory cytokines into the circulation mediated by CD14-mediated macrophages and monocytes. These cytokines eventually cause septic shock. Several in vitro and in vivo studies have shown that suppression of a CD14 function by a CD14 antibody led to an inhibition of the production of proinflammatory cytokines such as TNF-alpha, IL-1 beta, and IL-8. In the present study, we found that CD14 antisense oligonucleotide (ODN) can prevent lethal LPS shock in D-galactosamine-sensitized mice. This ODN inhibited CD14 expression in a mouse macrophage cell line, RAW264.7, and suppressed production of TNF-alpha in LPS-stimulated RAW264.7 cells. Furthermore, we designed a consensus antisense ODN that could hybridize human and mouse CD14 RNA, and we evaluated its efficacy. The consensus antisense ODN rescued mice primed with Mycobacterium bovis bacillus Calmette-Guerin (BCG) from the LPS-induced lethal shock. In this model, the CD14 antisense ODN down-regulated LPS-elicited CD14 expression in the liver, resulting in a decrease in LPS-induced TNF-alpha production. These findings suggest that the CD14 antisense ODN is distributed in the liver and efficiently suppresses LPS-induced TNF-alpha production by reducing CD14 expression on Kupffer cells. This CD14 antisense ODN may be useful for the development of a therapeutic agent against sepsis and septic shock. |
Keywords | sepsis TNF-? BCG(bacillus Calmette-Guerin) |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 105 |
End Page | 115 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332197 |
Web of Science KeyUT | 000168195700007 |
JaLCDOI | 10.18926/AMO/32006 |
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FullText URL | fulltext.pdf |
Author | Wani, Yoji| Notohara, Kenji| Tsukayama, Choutatsu| Okada, Shigeru| |
Abstract | We performed an immunohistochemical analysis of 2 major DNA mismatch repair proteins, human Mut L homologue-1 (hMLH1) and human Mut S homologue-2 (hMSH2), in hepatocellular carcinoma (HCC) using 33 biopsied and 58 surgically resected specimens, as well as 30 samples from non-cancerous livers. In well-differentiated HCCs, the immunoreactivity for these antigens was well preserved, and the staining intensity was stronger compared to the surrounding liver tissues. However, among 41 moderately-differentiated and 9 poorly-differentiated HCCs of the resected cases, hMLH1- and hMSH2-positive cells were significantly reduced in 19 (38%) and 9 (18%) cases, respectively. In 9 resected tumors, the expression of both of these antigens was reduced. Moreover, in 41 tumors of differing histological grades, 10 and 5 tumors for hMLH1 and hMSH2, respectively, contained a less-differentiated area with a reduced number of immunoreactive cells. The samples from non-cancerous biopsied liver and fetal autopsy tissue were well immunostained for both hMLH1 and hMSH2. We confirmed in this series that the hMLH1 and hMSH2 defect did commonly occur in high-grade HCCs, and that it might play a role in tumor progression. |
Keywords | hepatocellular carcinoma human Mut L homologue-1(hMLH1) human Mut S homologue-2(hMS2) mismatch repair proteins immunohistochemistry |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 65 |
End Page | 71 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332201 |
Web of Science KeyUT | 000168195700002 |
JaLCDOI | 10.18926/AMO/32005 |
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FullText URL | fulltext.pdf |
Author | Lalic, Hrvoje| Lekic, Andrica| Radosevic-Stasic, Biserka| |
Abstract | The genotoxic effects of occupational exposure to ionizing and non-ionizing radiation were investigated in 25 physicians and nurses working in hospitals and in 20 individuals working at radio-relay stations. Examination was conducted by chromosome aberration analysis of peripheral blood lymphocytes. The data showed that total number of chromosome aberrations in people exposed to ionizing and radio-frequency radiation (4.08 +/- 0.37 and 4.35 +/- 0.5 on 200 scored metaphases, respectively) were almost equally higher than those of non-irradiated subjects. The increase was in proportion to the number of individuals having more that 5-aberration/200 metaphases. Acentric fragments comprised the most frequently seen type of aberration. The average numbers in examined groups (11.8 x 10(-3) and 14.8 x 10(-3) per cell, respectively), were significantly higher than 4.2 x 10(-3), which was observed in controls, unexposed individuals. Dicentric fragments were also frequent (4.8 x 10(-3) and 6.25 x 10(-3), respectively, vs. 0.52 x 10(-3) in control). In contrast, the frequency of chromatid breaks increased only after ionizing radiation (3.8 x 10(-3) vs. 0.26 x 10(-3) in control). A positive correlation between the total number of chromosome aberrations and cumulative 6-years dosage was also found. The data emphasized the dangerous effects of prolonged exposure to both types of radiation and indicated that chromosomal aberration analysis should be obligatory for individuals working at radio-relay stations. |
Keywords | chromosomal aberrations ionizing radiation radiofrequency radiation |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 117 |
End Page | 127 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332198 |
Web of Science KeyUT | 000168195700008 |
JaLCDOI | 10.18926/AMO/32004 |
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FullText URL | fulltext.pdf |
Author | Kakehashi, Chikako| Mori, Masaharu| Kawabata, Teruyuki| Okada, Shigeru| |
Abstract | Administration of ferric nitrilotriacetate (Fe-NTA) in vivo causes acute renal tubular injury and finally induces renal cell carcinoma. There is accumulating evidence that these processes involve free radicals generated by Fe-NTA. To study the mechanism of renal carcinogenesis by Fe-NTA, we attempted to induce malignant transformation of primary cultured renal cells by treatment with Fe-NTA. When primary cultured renal cells (PRC) were treated continuously with Fe-NTA, all of the PRC died without transformation. On the other hand, when PRC were treated intermittently with Fe-NTA, transformed epithelial colonies were observed at 3 weeks after the first treatment. The established transformed cell line (RK523) showed drastic morphological transformation, grew in soft agar, and formed tumors when transplanted into athymic nude mice. These results indicate that the balance between cytotoxicity and mutagenecity is important for Fe-NTA induced transformation. The RK523 cell line may be a useful model for studying renal carcinogenesis in vitro. |
Keywords | renal cell Fe-NTA(ferric nitrilotriacetate) malignant transformation in vitro |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-04 |
Volume | volume55 |
Issue | issue2 |
Publisher | Okayama University Medical School |
Start Page | 97 |
End Page | 103 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11332205 |
Web of Science KeyUT | 000168195700006 |
JaLCDOI | 10.18926/AMO/32003 |
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FullText URL | fulltext.pdf |
Author | Yoshida, Yasuhiro| Higashi, Toshihiro| Nouso, Kazuhiro| Nakatsukasa, Harushige| Nakamura, Shin-ichiro| Watanabe, Akiharu| Tsuji, Takao| |
Abstract | Hepatic encephalopathy is one of the major complications in decompensated liver cirrhosis. The current study was conducted to clarify the mechanisms of zinc deficiency in liver cirrhosis and its involvement in hepatic encephalopathy via ammonia metabolism. Ten patients each with compensated or decompensated liver cirrhosis and 11 healthy volunteers were enrolled in the study. Serum zinc levels and its daily urinary excretion were measured, an oral zinc-tolerance test was performed to examine zinc malabsorption, and the effects of diuretics on zinc excretion and of zinc supplementation on ammonia metabolism in the skeletal muscle were studied. The mean serum zinc levels in patients with decompensated liver cirrhosis were found to be significantly lower than the levels in controls and patients with compensated liver cirrhosis. The serum zinc levels were inversely correlated with blood ammonia in the fasting state. In the oral zinc-tolerance test, the percent increase in serum zinc levels 120 and 180 min after ingestion was less in cirrhotic patients than in controls. A diuretic administration resulted in a significant reduction in serum zinc levels. An increased uptake of ammonia by and an increased release of glutamine from leg skeletal muscle after oral supplementation of zinc sulfate were evident. Taken together, zinc deficiency in decompensated cirrhotic patients appears to be due to low absorption and to high urinary excretion, for which excessive diuretic administration is, in part, responsible, and zinc supplementation might play an important role in the prevention of hepatic encephalopathy by activating glutamine synthetase. |
Keywords | zinc ammonia liver cirrhosis hepatic encephalopathy |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 349 |
End Page | 355 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779097 |
Web of Science KeyUT | 000172838400005 |
JaLCDOI | 10.18926/AMO/32002 |
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FullText URL | fulltext.pdf |
Author | Nakanishi, Tohru| Oka, Takashi| Akagi, Tadaatsu| |
Abstract | The structure of the human genome is almost completely elucidated and the life sciences will now aim for a general and integrated study of gene expressions and the functional elucidation of proteins. In such a study, various new techniques have been developed, and DNA microarray technology is the most representative one. As for the DNA microarray techniques, several thousands to tens of thousands of gene segments are immobilized on a glass slide at high density, and cDNA probes prepared from specific cells or tissues are hybridized on the slides from which gene expression profiles are obtained at one sweep in a short time. The present development of this technique and its possible application to medicine-related fields are described.</P> |
Keywords | DNA microarray DNA chip human genome embryonic stem(ES)cell single nucleotide polymorphism(SNP) |
Amo Type | Review |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 319 |
End Page | 328 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779093 |
Web of Science KeyUT | 000172838400001 |
JaLCDOI | 10.18926/AMO/32001 |
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FullText URL | fulltext.pdf |
Author | Takenami, Tatsuo| Sakaguchi, Kohsaku| Nishimura, Mamoru| Miyake, Yasuhiro| Miyashita, Manabi| Terao, Masako| Fujiwara, Akiko| Tsuji, Takao| |
Abstract | This study evaluated the effects of azathioprine in combination with low-dose prednisolone in the management of patients with intractable autoimmune hepatitis. Thirteen patients with intractable autoimmune hepatitis who had an incomplete or arrested response to conventional prednisolone therapy, or who relapsed during prednisolone maintenance therapy were additionally administered 50 or 100 mg/day of azathioprine in combination with prednisolone. This regimen reliably induced complete remission in 12 of 13 patients, and these 12 remained in remission during the follow-up period with maintenance therapy of 50 mg/day of azathioprine in combination with 5 mg/day of prednisolone. The findings of the current study indicate that the azathioprine and low-dose prednisolone combined therapy may offer a satisfactory alternative therapy for patients with intractable autoimmune hepatitis who have an incomplete or arrested response to conventional prednisolone therapy, or who relapse during prednisolone maintenance therapy. |
Keywords | autoimmune hepatitis azathioprine prednisolone |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 341 |
End Page | 347 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779096 |
Web of Science KeyUT | 000172838400004 |
JaLCDOI | 10.18926/AMO/32000 |
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FullText URL | fulltext.pdf |
Author | Matsuo, Masatsugu| Nishida, Keiichiro| Yoshida, Aki| Murakami, Takuro| Inoue, Hajime| |
Abstract | To clarify the involvement of the caspase family in the pathway of NO-induced chondrocyte apoptosis, osteoarthritis (OA) cartilage obtained from 8 patients undergoing total hip arthroplasty were used for histopathological study. Cartilage samples taken from non-fibrillated areas of femoral head resected during surgery for femoral neck fracture were used for comparison. DNA fragmentation of chondrocytes was detected by the nick end-labeling (TUNEL) method. Apoptosis was further confirmed by transmission electron microscopy. The distributions of nitrotyrosine (NT), caspase-3, and -9 were examined immunohistochemically. The populations of apoptotic as well as NT-, caspase-3-, and -9-positive cells were quantified by counting the number of cells in the superficial, middle, and deep layers, respectively. The TUNEL-positive cells were observed primarily in superficial proliferating chondrocytes, clustering chondrocytes, and deep-layer chondrocytes of OA cartilage. Few positive cells were seen in the proliferating chondrocytes in the middle layer. Positive reactions for caspase-3 and -9 were observed in chondrocytes in similar areas. Histological OA grade showed significant correlations with the mean populations of apoptotic chondrocytes (% apoptosis) over the 3 areas. The populations of NT-positive cells (% NT) over the same areas also showed significant correlation with OA grade. Positivity for caspase-3 closely correlated with the OA grade, % apoptosis and %NT. It was concluded that caspase-3 and -9 could play a role in NO-induced chondrocyte apoptosis in OA cartilage. |
Keywords | apoptosis caspase nitric oxide osteoarthritis chondrocyte |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 333 |
End Page | 340 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779095 |
Web of Science KeyUT | 000172838400003 |
JaLCDOI | 10.18926/AMO/31999 |
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FullText URL | fulltext.pdf |
Author | Koshima, Isao| |
Abstract | Recently, combined tissues or flaps have been used for the repair of extensively massive or wide defects resulting from radical wide resection. To further advance the development of combined tissue transfers, they should be reclassified. Based on our cases with free tissue transfers, we have created a new classification of combined flaps composed of "bridge", "chimeric", "siamese", "mosaic", and "chain-circle" flaps. The bridge flap is fabricated out together of separate flaps with short vascular pedicles. These form a compound flap supplied with a solitary vascular source. The chimeric flap is compounded from multiple different flaps but consists of only a single different tissue form. Each of the flaps is usually supplied by different branches from the same source vessel. It differs from the bridge flap in that the pedicle of each flap or tissue has some length for its movement for transfer. The siamese connected flap has 2 adjacent flaps that are simultaneously elevated, and a disparate vascular pedicle for each flap must be reestablished. This connected flap has double isolated pedicles. Themosaic connected flap consists of 2 adjacent flaps that are simultaneously elevated, and the pedicle of the distal flap is anastomosed to the pedicle branch of the proximal flap in the "bridge" fashion. The vascular pedicle of the proximal flap is anastomosed to a single vascular source. The chain-circle flap has 2 or more flaps like the bridge and chimeric flaps, and the distal end of the vascular source is anastomosed to the branch of the recipient vessel. Based on results with our patients, the lateral circumflex femoral system seems to be the most suitable candidate for the axial pedicle of these combined flaps, because the system has several branches of large and small caliber, and several tissue components, such as the vascularized ilium, rectus femoris muscle, gracilis muscle, lateral femoral cutaneous nerve, and fascia lata, are located nearby. |
Keywords | microsurgery free tissue transfer sombined flaps chimeric flap siamese flap mosaic flap chain-circle flap |
Amo Type | Review |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 329 |
End Page | 332 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779094 |
Web of Science KeyUT | 000172838400002 |
JaLCDOI | 10.18926/AMO/31998 |
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FullText URL | fulltext.pdf |
Author | Nakao, Atsunori| Sakagami, Kenichi| Mitsuoka, Shintaro| Uda, Masashi| Tanaka, Noriaki| |
Abstract | We report a case of retroperitoneal hematoma presenting as femoral nerve pulsy on antiplatelet therapy. The patient, a 78-year-old man who had undergone antiplatelet treatment using ticlopidine, was admitted to our hospital with complaints of sudden-onset low abdominal and back pain. Computed tomography showed an iso-density mass in the right retroperitoneum within the psoas muscle. We made a diagnosis of retroperitoneal hematoma compressing the femoral nerve and performed an operation to remove the hematoma in order to decompress the femoral neuropathy. Postoperatively, the patient rapidly recovered from the femoral neuropathy. In the particular case in which no antagonist against the ticlopidine is available, surgical decompression could produce a good outcome. |
Keywords | ticlopidine retroperitoneal hematoma |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 363 |
End Page | 366 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779099 |
Web of Science KeyUT | 000172838400007 |
JaLCDOI | 10.18926/AMO/31997 |
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FullText URL | fulltext.pdf |
Author | Akisu, Mete| Tuzun, Sevgi| Arslanoglu, Sertac| Yalaz, Mehmet| Kultursay, Nilgun| |
Abstract | In the present investigation, we studied the effect of recombinant human erythropoietin (r-HuEPO) on serum malondialdehyde (MDA) as an index of lipid peroxidation, related to iron-catalyzed free radical reaction and erythrocyte superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) activities in very-low-birth weight (VLBW) infants. Forty premature infants, at gestational ages were less than 33 weeks and birthweights were less than 1,500 g, were enrolled in the study. The study population was randomly divided into 2 groups. Twenty infants in Group 1 (treatment group) were given r-HuEPO, and 20 infants in Group 2 served as the control. r-HuEPO treatment (750 U/kg a week) was initiated on the 10th day of life and continued for 6 weeks. Preterm infants given erythrocyte transfusions during the study were excluded from the results. Serum ferritin and MDA levels, and erythrocyte superoxide dismutase (SOD), catalase (CAT), and glutathione peroxidase (GPX) activities were analyzed at the end of the first week of life (at the beginning of the study). Subsequently, serum ferritin, and MDA levels were measured at the end of the 3rd and the 6th week. SOD, CAT, and GPX activities in the hemolysate were analyzed at the end of the 4th week. Six infants in the control group and 1 infant in the r-HuEPO group received transfusions through the end of the study, and these infants were excluded from the results. Significantly decreased serum ferritin concentrations were found in the r-HuEPO group compared to those in the control group both at the end of the 3rd and the 6th week (P < 0.05, and P < 0.01, respectively). In addition, serum MDA levels were also significantly reduced in Group 1 compared to control both at the end of the 3rd and the 6th week (P < 0.01 and P < 0.05, respectively). A good correlation was found between serum MDA and ferritin levels in Group 1. When the 2 groups were compared with respect to activities of SOD, CAT, and GPX at the end of the 4th week, no differences were observed. Our findings in this study show that administration of r-HuEPO significantly decreases lipid peroxidation, but does not affect erythrocyte antioxidant enzyme(s) activities in preterm infants. The mechanism responsible for the r-HuEPO-induced decrease in lipid peroxidation may concern inhibition to iron-catalyzed free radical reactions.</P> |
Keywords | anemia of prematurity erythropoietin lipid peroxidation superoxide dismutase catalase glutathione peroxidase |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-12 |
Volume | volume55 |
Issue | issue6 |
Publisher | Okayama University Medical School |
Start Page | 357 |
End Page | 362 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11779098 |
Web of Science KeyUT | 000172838400006 |
JaLCDOI | 10.18926/AMO/31996 |
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FullText URL | fulltext.pdf |
Author | Yumite, Yasuamasa| Takeuchi, Kazuhiro| Harada, Yoshiaki| Ogawa, Norio| Inoue, Hajime| |
Abstract | We studied total nitric oxide (nitrite + nitrate) (NO) levels in cerebrospinal fluid (CSF) of chronic spinal diseases in nonsmokers (133 patients: 76 men and 57 women; mean age, 63 years; range, 15-92 years) by the Griess method to clarify the role of NO in different spinal diseases. The extent of compression in terms of numbers of disc level at the compressed spinal nerve and neurological evaluation were also assessed according to the Japanese Orthopaedic Association scores. The spinal diseases included cervical myelopathy and radiculopathy (cervical disease group), ossification of yellow ligament (thoracic disease group), and lumbar disc herniation, lumbar canal stenosis and lumbar spondylolisthesis (lumbar disease group). NO levels in the spinal disease groups (4.98+/-2.28 micromol/l: mean +/- SD) were significantly higher than that in the control group (2.53+/-0.94 micromol/l). An inverse correlation was detected between the elevated levels of NO and the grade of clinical symptoms in the cervical disorders. The number of disc level at the compressed spinal nerve was positively correlated with elevated NO levels in CSF in the cervical and lumbar disorder groups. These results indicate that nerve compression may elevate NO levels in CSF, and that NO concentration in the CSF might be a useful marker of damage to nervous system in spinal disorders. |
Keywords | Griess method Japanese Orthopaedic Association Score(JOA score) magnetic resonance imaging(MRI) biochemistry assay |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-08 |
Volume | volume55 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 219 |
End Page | 228 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11512564 |
Web of Science KeyUT | 000170367200004 |
JaLCDOI | 10.18926/AMO/31994 |
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FullText URL | fulltext.pdf |
Author | Aono, Hiroshi| Hirakawa, Masahisa| Unruh, Gregory K| Kindscher, James D| Goto, Hiroshi| |
Abstract | The mechanisms of arterial hypotension following intravenous anesthetic induction agents are multifactorial. The purpose of this study was to evaluate and compare the effects of thiopental, propofol and etomidate on hemodynamics, sympathetic outflow and arterial baroreflex sensitivity using not only neuraxis-intact but also totally baro-denervated rabbits. A total of 60 rabbits was anesthetized with urethane, tracheotomized, and mechanically ventilated with oxygen in nitrogen (FiO2 0.5). The left renal sympathetic nerve was isolated and placed on a bipolar electrode to record renal sympathetic nerve activity (RSNA). Thirty animals underwent a surgical preparation of total baroreceptor denervation. Bolus injections of an anesthesia induction dose of thiopental 4 mg/kg and twice the induction dose of propofol 4 mg/kg significantly decreased RSNA to the same extent (19.4+/-6.7 and 19.7+/-5.2% reduction, mean +/- SEM) and mean arterial pressure (MAP) also to the same extent (19.5+/-4.6 and 22.1+/-3.1% reduction) in the neuraxis-intact animals. RSNA was increased (34.5+/-6%) without reduction of MAP by an induction dose of etomidate, 0.3 mg/kg. Sympathetic barosensitivity was attenuated even 10 min after thiopental at 4 mg/kg or propofol at 4 mg/kg (68% and 54% of control, respectively). Propofol at 2 mg/kg (induction dose) and etomidate at 0.6 mg/kg decreased RSNA and MAP only in the baro-denervated animals. It was found from the barosensitivity study that patients can be hemodynamically unstable even though blood pressure has returned to normal after thiopental and propofol administration. Data suggest that etomidate can even stimulate the sympathetic nervous system and increase sympathetic outflow. It was also clearly found from the baro-denervated animal study that thiopental was stronger than propofol in directly suppressing sympathetic outflow at the induction dose. |
Keywords | intravenous anesthetics sympathetic outflow baroreflex |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-08 |
Volume | volume55 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 197 |
End Page | 203 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11512561 |
Web of Science KeyUT | 000170367200001 |
JaLCDOI | 10.18926/AMO/31993 |
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FullText URL | fulltext.pdf |
Author | Coskun, Senol| Yuksel, Hasan| Bilgi, Yasar| Lacin, Selman| Tansug, Nermin| Onag, Ali| |
Abstract | Postnatal adaptations of cardiac hemodynamics in infants born vaginally or by caesarean section may be different. These cardiac functions were evaluated by Doppler echocardiography to assess adaptation differences. Cardiac output, heart rate, stroke volume, mean arterial pressure, total systemic vascular resistance, ejection fraction, and ductus arteriosus diameter were determined and compared at 1, 24 and 72 h of life in 22 infants born vaginally (group 1) and 23 born by caesarean section (group 2). One hour after delivery, heart rate, mean blood pressure, and total systemic resistance were found to be higher in group 1 infants (P < 0.01, P < 0.05, P < 0.05 respectively). Stroke-volume measurements were significantly higher in group 2 (P < 0.05). The ejection fraction and cardiac output values were similar in both groups. At 24 and 72 h, no significant differences were observed in measurements of infants born vaginally or by caesarean section. We did not find a parameter negatively affecting healthy newborns in either mode of delivery. However, under pathological conditions affecting the cardiovascular system at 1 h of life, including perinatal infections and hypoxemia, a lower stroke volume, higher heart rate, higher mean blood pressure, and higher peripheral resistance may cause additional work load to the cardiovascular system in infants born vaginally. |
Keywords | newborn Doppler echocardiography vaginal delivery caearean section |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-08 |
Volume | volume55 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 213 |
End Page | 218 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11512563 |
Web of Science KeyUT | 000170367200003 |
JaLCDOI | 10.18926/AMO/31992 |
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FullText URL | fulltext.pdf |
Author | Nakao, Atsunori| Iwagaki, Hiromi| Notohara, Kenji| Morimoto, Yushinori| Ariki, Norifumi| Kanagawa, Taiichiro| Isozaki, Hiroshi| Tanaka, Noriaki| |
Abstract | A 69-year-old woman was admitted to our hospital because of anal bleeding and fatigue. The patient was previously diagnosed as having Evans' syndrome on the basis of hematological examination and had been treated with predonisolone for 8 years. On admission, severe anemia and thrombocytopenia were noted. Colonoscopy and Barium enema studies demonstrated an irregular tumor with hemorrhagic ulceration in the rectum, which was histopathologically confirmed as an adenocarcinoma. After red blood cells and platelets were transfused, and the patient was treated with high-dose gammaglobulin, predonisolone, and camostat mesylate, the platelet count gradually increased and hemolysis was well controlled. The patient then underwent Hartmann's operation and splenectomy without any postoperative complications. Predonisolone and high-dose immunoglobulin therapy in a rectal cancer burdened patient with Evans' syndrome is considered useful in combination with surgical treatment. This is the first case report of rectal carcinoma resection in a patient with Evans' syndrome. |
Keywords | immune thrombocytopenia autoimmune hemolytic anemia surgical treatment |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-08 |
Volume | volume55 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 253 |
End Page | 257 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11512568 |
Web of Science KeyUT | 000170367200008 |
JaLCDOI | 10.18926/AMO/31990 |
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FullText URL | fulltext.pdf |
Author | Togami, Izumi| Sasai, Nobuya| Tsunoda, Masatoshi| Sei, Tetsuro| Yabuki, Takayuki| Kitagawa, Takahiro| Mitani, Masahiko| Akaki, Shiro| Kuroda, Masahiro| Hiraki, Yoshio| |
Abstract | A preliminary study was conducted to evaluate the superior and inferior glenoid labra with abductive movement using an open-type MR unit in asymptomatic healthy volunteers. Both fast low angle shot (FLASH) and turbo spin echo (TSE) images were obtained to evaluate the shapes of both the superior and inferior labra, as well as to assess changes in signal at these sites. As the abduction angle was increased, the shape of the superior labrum changed from round or triangular to crescentic and a higher signal was frequently seen. At an abduction angle of 150 degrees, an increase in signal was seen in one-half of the superior labra; this increase was noted more frequently in volunteers over 40 years of age. In some of the superior labra, the increase in signal seen at 150 degrees abduction disappeared on subsequent images obtained at 0 degrees abduction. Hence, the increase in signal was considered to be a reversible change. The shape of the inferior labrum tended to change from crescentic to triangular or round. An increase in signal in the inferior labrum was unrelated to the abduction angle. Abductive kinematic studies using an open-type MR unit provides information about the morphology of the superior and inferior labra, as well as information about signal changes occurring at these sites. |
Keywords | shoulder kinematic magnetic resonance imaging(MRI) glenoid labrum open-type MRI |
Amo Type | Article |
Publication Title | Acta Medica Okayama |
Published Date | 2001-08 |
Volume | volume55 |
Issue | issue4 |
Publisher | Okayama University Medical School |
Start Page | 237 |
End Page | 243 |
ISSN | 0386-300X |
NCID | AA00508441 |
Content Type | Journal Article |
language | English |
File Version | publisher |
Refereed | True |
PubMed ID | 11512566 |
Web of Science KeyUT | 000170367200006 |